Write the structure of the major organic product in each of the following reaction:
$\text{CH}_3\text{CH}_2\text{Br}+\text{KCN}\xrightarrow{\text{aq. ethanol}}$
$\text{CH}_3\text{CH}_2\text{Br}+\text{KCN}\xrightarrow{\text{aq. ethanol}}$
Download our app for free and get started
$\text{CH}_3\text{CH}_2\text{Br}+\text{KCN}\xrightarrow[(\text{Nucleophilic substitution})]{\text{aq. ethanol}} \text{CH}_3\text{CH}_2\text{CN}+\text{KBr}\\\text{Bromobutane}\ \ \ \ \ \ \ \ \ \ \ \ \ \ \ \ \ \ \ \ \ \ \ \ \ \ \ \ \ \ \ \ \ \ \ \ \ \ \ \ \ \ \ \ \ \ \ \ \ \ \ \text{Cyanoethane}$
Download our appand get started for free
Experience the future of education. Simply download our apps or reach out to us for more information. Let's shape the future of learning together!No signup needed.*
Similar Questions
- 1Write the $\ce{IUPAC}$ name of the following compound: $\ce{CH_2 = CHCH_2Br}.$View Solution
- 2View SolutionWrite the structures of the following organic halogen compound.
1-Bromo-4-sec-butyl-2-methylbenzene. - 3View SolutionGive the IUPAC name of the following compound:
- 4View SolutionHow the following conversion can be carried out?
Benzene to diphenyl. - 5Which would undergo $S_N2$ reaction faster in the following pair:View Solution
- 6View SolutionHalogen compounds used in industry as solvents are alkyl chlorides rather than bromides and iodides. Give reason for your answer.
- 7View SolutionGive reasons for the following:
Iodoform is obtained by reaction of acetone with hypoiodite ion but not iodide ion. - 8View SolutionPredict the major product formed when 2-Bromopentane reacts with alcoholic KOH.
- 9View SolutionOut of chlorobenzene and benzyl chloride, which one gets easily hydrolysed by aqueous NaOH and why?
- 10View SolutionHow the following conversion can be carried out?
2-Methyl-1-propene to 2-chloro-2-methylpropane.